CRO Services - ACTG-CRO
Each Clinical Trial requires its own individualized monitoring plan: particular complexity, therapeutic criticality, end points' data, the conduct and processes at each site and compliance.
At ACTG-CRO, we transform on-site monitoring reactive approach into a quality risk management proactive approach by using monitoring strategies to ensure oversight to what is not prevented via protocol or eCRF design.
The documentation of adverse events is carried out according to the ICH/GCP guidelines in relation with the investigators.
Clinical Research, Tunisia, Africa, Clinical Trials, CRA, SCRA, Clinical Research Associate, GCP, Monitor, Monitoring, Senior Clinical Research Associate, CRA I, CRA II, CRA III, LCRA, Oncology, Cardiovascular, Neuroscience, Immunology, Infectious Diseases, Metabolism, Field Based, Home Based, CRO, Pharmaceutical